System For Hydrating Defibrillation Electrodes

ABSTRACT

According to an aspect of the present disclosure, an automated external defibrillator is configured to deliver one or both of electrical pulses and shocks to a heart of a patient during a cardiac emergency. The defibrillator includes a defibrillator electrode delivery system and a hydrating system. The defibrillator electrode delivery system includes a pair of defibrillation electrode pads. Each pad supports a hydrogel to facilitate the deliverance of one or both of electrical pulses and shocks to a patient. The hydrating system includes a fluid container that maintains a fluid that hydrates the hydrogel over a predetermined time period to prolong the effectiveness of the hydrogel.

BACKGROUND

1. Technical Description

The present disclosure relates to defibrillators and defibrillationelectrodes and, more particularly, to systems and methods for hydratingdefibrillation electrodes connected to a defibrillator prior to theelectrodes being used on a patient.

2. Background of Related Art

In many instances, when an emergency situation arises at a publiclocation remote from a medical facility, Automated ExternalDefibrillators (AED's) may generally be available for use on theindividual experiencing the medical emergency. An AED is a portableelectronic device that automatically diagnoses the potentially lifethreatening cardiac arrhythmias of ventricular fibrillation andventricular tachycardia in a patient, and is able to treat them throughdefibrillation, the application of electrical therapy which stops thearrhythmia, allowing the heart to reestablish an effective rhythm.

Like many other medical devices, AED's include electrodes that generallyhave a conductor portion that is often covered or coated in a conductivegel/hydrogel to enhance the ability of the electrode to adhere to apatient's skin. However, an AED may be stored for prolonged periodswhich may cause the conductive gel/hydrogel to become dry to the pointwhere its effectiveness is altered or compromised. In this respect, whenan AED is stored for long periods of time, the conductive gel/hydrogelmay lose its ability to adhere to a patient or may demonstrateexcessively high contact impedance which, if used on a patient, canresult in the patient being burned.

Thus, a need exists for a system that prolongs the lifespan of theconductive gel/hydrogel used with defibrillation electrodes to minimizerisks associated with AEDs that will be stored for long periods of time.

SUMMARY

According to one aspect, an automated external defibrillator isconfigured to deliver electrical pulses and/or shocks to a heart of apatient during a cardiac emergency. The defibrillator includes adefibrillator electrode delivery system and a hydrating system. Thedefibrillator may include a controller operatively coupled to one orboth of the defibrillator electrode delivery system and the hydratingsystem.

The defibrillator electrode delivery system includes a pair ofdefibrillation electrode pads and an energy source. Each pad supports ahydrogel to facilitate the deliverance of electrical pulses and/orshocks to a patient. Each defibrillation electrode pad is electricallycoupled to the energy source to selectively enable the deliverance ofelectrical pulses and/or shocks to a patient. One or both of thedefibrillation electrode pads are fixedly electrically coupled to theenergy source.

The hydrating system includes a fluid container. The fluid containermaintains a fluid that hydrates the hydrogel over a predetermined timeperiod to prolong the effectiveness of the hydrogel. The fluid may bewater.

The hydrating system may include a mesh supported on the fluid containerThe mesh may define a plurality of micro pores. The pair ofdefibrillation electrode pads may be supported on the mesh.

The hydrating system may include a sprayer configured to spray one orboth of the defibrillation electrode pads with the fluid. The sprayermay be configured to periodically spray one or both of thedefibrillation electrode pads with the fluid. The hydrating system mayinclude a plurality of sprayers. Each sprayer may be configured to sprayone or both of the defibrillation electrode pads with the fluid.

According to another aspect, an automated external defibrillator isconfigured to deliver electrical pulses and/or shocks to a heart of apatient during a cardiac emergency. The defibrillator includes ahousing, a pair of defibrillation electrode pads, and a hydratingsystem. A controller maybe supported by the housing that is operativelycoupled to the hydrating system.

The housing supports an electrical connector, a battery, and highvoltage circuitry.

The pair of defibrillation electrode pads are supported on the housing.Each defibrillation electrode pad supports a hydrogel and ispre-connected to the electrical connector of the housing so that eachdefibrillation electrode pad is in electrical communication with thebattery and the high voltage circuitry.

The hydrating system includes a fluid container within the housing. Thehousing may include the fluid container. The fluid container maintains afluid that hydrates the hydrogel to prolong the effectiveness of thehydrogel. The fluid may be water. The hydrating system may include amesh supported on the fluid container. The mesh may be supported on thehousing. The mesh is in fluid communication with the fluid container.The pair of defibrillation electrode pads may be supported on the mesh.

The hydrating system may include a sprayer configured to spray one orboth of the defibrillation electrode pads with the fluid. The sprayermay be configured to periodically spray one or both of thedefibrillation electrode pads with the fluid. The hydrating system mayinclude a plurality of sprayers. Each sprayer maybe configured to sprayone or both of the defibrillation electrode pads with the fluid.

According to yet another aspect, a method of preserving a defibrillationelectrode pad of an automated external defibrillator involves the stepof providing an automated external defibrillator including adefibrillation pad and a hydrating system where the defibrillation padsupports a hydrogel. The method includes hydrating the hydrogel of thedefibrillation pad with the hydrating system of the automated externaldefibrillator while storing the automated external defibrillator.

BRIEF DESCRIPTION OF THE DRAWINGS

Various embodiments of the presently disclosed systems are describedherein with reference to the drawings wherein:

FIG. 1 is a top, plan schematic view of an exemplary automated externaldefibrillator;

FIG. 2 is a side, elevational schematic view of an automated externaldefibrillator according to an embodiment of the present disclosure;

FIG. 3 is a side, elevational schematic view of the automated externaldefibrillator illustrated in FIG. 2, after a predetermined time period;

FIG. 4 is a side, elevational schematic view of an automated externaldefibrillator shown in a first condition according to another embodimentof the present disclosure; and

FIG. 5 is a side, elevational schematic view of the automated externaldefibrillator illustrated in FIG. 4 shown in a second condition.

DETAILED DESCRIPTION

Embodiments of the presently disclosed automated external defibrillatorswill now be described in detail with reference to the drawing figureswherein like reference numerals identify similar or identical elements.

As illustrated in FIG. 1, an exemplary automated external defibrillatoris generally designated as 100. Automated external defibrillator 100 isconfigured to deliver electrical pulses and/or shocks to a heart of apatient during a cardiac emergency. Automated external defibrillator 100includes a housing 102 and an electrode delivery system 110 supported byhousing 102. Electrode delivery system 110 is configured to generate anddeliver electrical pulses and/or shocks (e.g., manually and/orautonomously as appreciated by one skilled in the art). Electrodedelivery system 110 includes a controller 112, an energy source 114(e.g., a battery), and circuitry 116 in electrical communication withcontroller 112 and energy source 114. Circuitry 116 may be configuredfor high voltage compatibility. Notably, any suitable combination ofconductors, resistors, transistors, capacitors, inductors, etc. may beused to electrically couple any of the presently disclosed componentsdescribed herein.

With continuing reference to FIG. 1, electrode delivery system 110includes a pair of electrode pads 120 that are electrically coupled tocontroller 112 and/or energy source 114 via lead wires 122 and anelectrical connector 124 supported on or in electrical communicationwith a first end of lead wires 122. In this regard, electrical connector124 electrically couples lead wires 122 and circuitry 116 toelectrically couple controller 112 and/or energy source 114 to electrodepads 120 to deliver electrical pulses and/or shocks. The pair ofelectrode pads 120 are supported on or in electrical communication witha second end of lead wires 122.

As illustrated in FIGS. 2-3, an automated external defibrillatoraccording to one embodiment of the present disclosure is generallyreferred to as 200. Automated external defibrillator 200 is similar toautomated external defibrillator 100 and is described herein only to theextent necessary to describe the differences in construction andoperation thereof. Automated external defibrillator 200 includes ahousing 202 that supports an electrode delivery system 110 and ahydrating system 210. Electrode pads 120 are pre-connected to controller112 and/or energy source 114 such that electrode pads 120 are inelectrical communication with controller 112 and/or energy source 114.Electrode pads 120 may be fixedly pre-connected to controller 112 and/orenergy source 114. In order to facilitate the deliverance of electricalpulses and/or shocks to a patient, a hydrogel 120 a (or other suitablematerial; e.g., a foam) is supported on electrode pads 120 of electrodedelivery system 110. Hydrogel 120 a enhances the ability of electrodepads 120 to adhere to a patient's skin when delivering electrical pulsesand/or shocks generated by controller 112 and/or energy source 114.

With continuing reference to FIGS. 2-3, hydrating system 210 isconfigured to reduce a moisture vapor transmission rate (i.e., tendencyto dry-out) of hydrogel 120 a of electrode pads 120 without the need forspecial packaging of electrode pads 120. In this regard, electrode pads120 may be pre-connected to controller 112 and/or energy source 114 tohasten the usability of electrode pads 120 by eliminating the need toopen packaging and and/or the need to electrically connect electrodepads 120 to controller 112 and/or energy source 114 at the time of acardiac emergency.

As depicted in FIGS. 2-3, hydrating system 210 includes a fluidcontainer 230 and a mesh 240 overlying fluid container 230. Fluidcontainer 230 may be supported on and/or within housing 202. A fluid “F”(e.g., water, saline, etc.) suitable to hydrate hydrogel 120 a ofelectrode pads 120 is contained in fluid container 230. Mesh 240 may besupported on housing 202 and/or fluid container 230 such that mesh 240is disposed in fluid communication with fluid “F” to enable thehydration of hydrogel 120 a over a predetermined time period, whenelectrode pads 120 are supported on mesh 240, to prolong theeffectiveness of hydrogel 120 a. In particular, fluid “F” from container230, hydrates hydrogel 120 a of electrode pads 120.

In an embodiment, mesh 240 may include a plurality of micro pores 242 tofacilitate hydration of hydrogel 120 a. It is contemplated that mesh 240may include an fluid permeable material and may be selected such that apredetermined rate of fluid transfer is obtained therethrough that issufficient to maintain hydrogel 120 a at least substantially hydrated.

As appreciated, after a predetermined time period, fluid “F” willdiminish (see FIG. 3) as fluid “F” hydrates hydrogel 120 a. In thisregard, a refill conduit 250 may be disposed in fluid communication withfluid container 230 to enable one to refill and/or re-change fluidcontainer 230 with fluid “F.”

Turning now to FIGS. 4-5, an automated external defibrillator accordingto another embodiment of the present disclosure is generally referred toas 300. Automated external defibrillator 300 is similar to automatedexternal defibrillators 100 and 200 and is described herein only to theextent necessary to describe the differences in construction andoperation thereof. Automated external defibrillator 300 includes ahousing 302 that supports an electrode delivery system 110 and ahydrating system 310 for hydrating a hydrogel 120 a supported onelectrode pads 120 of electrode delivery system 110.

With continuing reference to FIGS. 4-5, hydrating system 310 is alsoconfigured to reduce a moisture vapor transmission rate of hydrogel 120a of electrode pads 120 without the need for special packaging ofelectrode pads 120. Hydrating system 310 includes a fluid container 330and a sprayer system 332 with one or more sprayers 332 a. Sprayer system332 may be operably coupled to controller 112. Fluid container 330 maybe supported on and/or within housing 302. A fluid “F”, suitable tohydrate hydrogel 120 a of electrode pads 120, is supported in fluidcontainer 330 and may be sprayed (see FIG. 5) via one or more sprayers332 a of sprayer system 332 directly or indirectly onto hydrogel 120 aof electrode pads 120 to hydrate hydrogel 120 a over a predeterminedtime period to prolong the effectiveness of the hydrogel 120 a whenelectrode pads 120 are disposed adjacent sprayers 332 a. In particular,sprayer system 332, may include any suitable mechanical, chemical, andor electrical component such as a motor (not shown) and/or controllerthat is operatively coupled to controller 112 to spray fluid “F” fromsprayers 332 a. Notably, sprayer system 332 may include independentcomponents such as a controller, energy source, etc. to operate sprayersystem 332 independent of electrode delivery system 110. Sprayer system332 may be configured to continuously spray, to spray at periodicintervals, and/or to spray at random intervals. To this end, anysuitable spray pattern and timing thereof is contemplated. Similar torefill conduit 250 above, a refill conduit 350 may be secured to sprayersystem 332 to enable one to refill and/or change fluid “F” within fluidcontainer 330.

Electrode pads configured for use with any of the automated externaldefibrillators disclosed herein are shown and described in InternationalPatent Application Serial No. PCT/US2007/010060, filed Apr. 27, 2007(International Publication No. WO 2007/0127266); in U.S. patentapplication Ser. No. 12/237,803, filed on Sep. 25, 2008 (U.S. PatentApplication Publication No. 2010/0072060); and U.S. patent applicationSer. No. 12/043,266, filed on Mar. 6, 2008 (U.S. Patent ApplicationPublication No. 2009/0227857), the entire content of each of which beingincorporated herein by reference.

An example of a suitable polymer which may be utilized in the electrodepads disclosed herein includes RG-73P4 hydrogel, commercially availablefrom Tyco Healthcare Group d/b/a/ Covidien. Other suitable hydrogelsinclude those disclosed in U.S. patent application Ser. No. 12/261,122,filed on Oct. 30, 2009 (U.S. Patent Application Publication No.2009/0270709); and U.S. patent application Ser. No. 12/261,134, filed onOct. 30, 2009 (U.S. Patent Application Publication No. 2009/0270710),the entire disclosures of each of which are incorporated herein byreference.

It is to be understood that the foregoing description is merely adisclosure of particular embodiments and is in no way intended to limitthe scope of the disclosure. Other possible modifications will beapparent to those skilled in the art and are intended to be within thescope of the present disclosure.

1. An automated external defibrillator configured to deliver electricalpulses and/or shocks to a heart of a patient during a cardiac emergency,the defibrillator comprising: a defibrillator electrode delivery systemincluding a pair of defibrillation electrode pads, each pad supporting ahydrogel to facilitate the deliverance of electrical pulses and/orshocks to the patient; and a hydrating system including a fluidcontainer and a sprayer, the fluid container maintaining a fluid, thesprayer configured to periodically spray at least one of thedefibrillation electrode pads with the fluid to prolong theeffectiveness of the hydrogel. 2-4. (canceled)
 5. The defibrillatoraccording to claim 1, wherein the fluid is water.
 6. The defibrillatoraccording to claim 1, wherein the defibrillator electrode deliverysystem includes an energy source, each defibrillation electrode padbeing electrically coupled to the energy source to selectively enablethe deliverance of electrical pulses and/or shocks to a patient.
 7. Thedefibrillator according to claim 6, wherein at least one of thedefibrillation electrode pads are fixed electrically coupled to theenergy source.
 8. (canceled)
 9. The defibrillator according to claim 1,wherein the sprayer is configured to periodically spray at least one ofthe defibrillation electrode pads with the fluid.
 10. The defibrillatoraccording to claim 1, wherein the hydrating system includes a pluralityof sprayers, each sprayer configured to spray at least one of thedefibrillation electrode pads with the fluid.
 11. The defibrillatoraccording to claim 1, further comprising a controller operativelycoupled to at least one of the defibrillator electrode delivery systemand the hydrating system.
 12. An automated external defibrillatorconfigured to deliver electrical pulses and/or shocks to a heart of apatient during a cardiac emergency, the defibrillator comprising: ahousing supporting an electrical connector, a battery, and high voltagecircuitry; a pair of defibrillation electrode pads supported on thehousing, each defibrillation electrode pad supporting a hydrogel andbeing pre-connected to the electrical connector of the housing so thateach defibrillation electrode pad is in electrical communication withthe battery and the high voltage circuitry; and a hydrating systemincluding a fluid container and a sprayer within the housing, the fluidcontainer maintaining a fluid, the sprayer configured to spray at leastone of the defibrillation electrode pads with the fluid to prolong theeffectiveness of the hydrogel. 13-16. (canceled)
 17. The defibrillatoraccording to claim 12, wherein the fluid is water.
 18. (canceled) 19.The defibrillator according to claim 12, wherein the sprayer isconfigured to periodically spray at least one of the defibrillationelectrode pads with the fluid.
 20. The defibrillator according to claim12, wherein the hydrating system includes a plurality of sprayers, eachsprayer configured to spray at least one of the defibrillation electrodepads with the fluid.
 21. The defibrillator according to claim 12,further comprising a controller supported by the housing and beingoperatively coupled to the hydrating system.
 22. (canceled)